| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:28108127-28108396 | Common:1; Rare:79 | ||||
| chr11:31369732-31369891 | Rare:47 | ||||
| chr11:31509577-31509793 | Common:1; Rare:68 | ||||
| chr11:33161433-33161648 | Common:6; Rare:59 | ||||
| chr11:34052143-34052372 | Common:2; Rare:106 | ||||
| chr11:34916248-34916578 | Common:9; Rare:135; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr11:35138949-35139212 | Common:1; Rare:59 | ||||
| chr11:35525552-35525894 | Common:1; Rare:84 | ||||
| chr11:36510258-36510353 | Rare:28 | ||||
| chr11:46700559-46700818 | Common:1; Rare:66 | ||||
| chr11:46700947-46701082 | Common:1; Rare:44 | ||||
| chr11:46846235-46846422 | Common:1; Rare:55 | ||||
| chr11:47214843-47215123 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248788-47248947 | Rare:66 | ||||
| chr11:47578945-47579141 | Rare:103; Clinvar:2; Clinvar (pathogenic):1 |